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2,4,5-Trimethyloxazole

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Identification
Molecular formula
C6H9NO
CAS number
14611-52-0
IUPAC name
2,4,5-trimethyloxazole
State
State

At room temperature, 2,4,5-Trimethyloxazole is a liquid.

Melting point (Celsius)
-39.00
Melting point (Kelvin)
234.15
Boiling point (Celsius)
142.00
Boiling point (Kelvin)
415.15
General information
Molecular weight
111.14g/mol
Molar mass
111.1440g/mol
Density
0.9780g/cm3
Appearence

2,4,5-Trimethyloxazole typically appears as a clear liquid. It can have a mild characteristic odour, which may be similar to other oxazole derivatives.

Comment on solubility

Solubility of 2,4,5-Trimethyloxazole

2,4,5-trimethyloxazole, with its unique chemical structure, presents interesting solubility characteristics. Generally, the solubility of a compound can depend on various factors such as the solvent used, temperature, and the molecular interactions between solute and solvent. Here are some key points regarding its solubility:

  • Polar vs. Non-Polar Solvents: 2,4,5-trimethyloxazole is expected to be more soluble in polar solvents, such as water and methanol, due to the presence of polar functional groups.
  • Hydrogen Bonding: The ability to form hydrogen bonds can enhance solubility; in this case, the oxazole ring might participate in such interactions.
  • Temperature Dependence: Like many organic compounds, solubility can increase with temperature, suggesting that heating the solvent may help dissolve 2,4,5-trimethyloxazole more effectively.
  • Concentration Effects: At higher concentrations, the solubility might decrease due to solute-solute interactions, which can lead to decreased effective dissolution.

In summary, the solubility of 2,4,5-trimethyloxazole is influenced by a variety of factors, with polarity and temperature playing crucial roles. Understanding these elements is essential for practical applications involving this compound.

Interesting facts

Interesting Facts about 2,4,5-Trimethyloxazole

2,4,5-trimethyloxazole is a fascinating nitrogen-containing heterocyclic compound that has garnered attention in various fields, particularly in medicinal chemistry and organic synthesis. Here are some key insights:

  • Structural Versatility: The presence of multiple methyl groups in its structure contributes to its unique reactivity and stability. This structural feature also allows the compound to engage in diverse reactions, making it a valuable building block in organic synthesis.
  • Biological Implications: Compounds like 2,4,5-trimethyloxazole have been studied for their potential bioactivity, particularly as antimicrobial agents. The oxazole ring system is known for its role in several biologically active compounds.
  • Applications in Material Science: Due to its properties, this compound may find applications in the creation of specialized polymers or materials, highlighting the intersection between chemistry and material science.
  • Research Interest: Ongoing research continues to explore the compound's applications, creating an exciting area of study for both chemists and pharmacologists. As one scientist quipped, "With every methyl group, there lies a new opportunity for discovery!"

In summary, 2,4,5-trimethyloxazole is not just another compound; it represents a gateway to understanding more complex organic reactions and pharmacological effects. Its distinctive features contribute to an array of potential applications, emphasizing the importance of heterocycles in scientific innovation.

Synonyms
2,4,5-TRIMETHYLOXAZOLE
20662-84-4
Trimethyloxazole
Oxazole, trimethyl-
2,4,5-Trimethyl-1,3-oxazole
Oxazole, 2,4,5-trimethyl-
trimethyl-1,3-oxazole
EINECS 243-952-4
B04PF51WXI
TRIMETHYLOXAZOLE [FHFI]
DTXSID0022274
FEMA NO. 4394
DTXCID302274
FEMA 4394
243-952-4
RefChem:442800
MFCD00005308
Oxazole, 2,4,5-trimethyl
2,4,5-Trimethyl oxazole
UNII-B04PF51WXI
Trimethyl-Oxazole
2,4,5-trimethyl-oxazole
SCHEMBL76903
SCHEMBL295280
SCHEMBL3737128
SCHEMBL5536771
SCHEMBL5640724
2,4,5-Trimethyloxazole, 95%
CHEBI:179309
2,4,5-Trimethyl-1,3-oxazole #
2,4,5-Trimethyloxazole, 99%, FG
AKOS015900489
DS-3980
FT35627
DB-045329
CS-0153589
NS00021839
T2595
Q27274214
InChI=1/C6H9NO/c1-4-5(2)8-6(3)7-4/h1-3H